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CISD2 gene

Known as: NUTRIENT DEPRIVATION AUTOPHAGY FACTOR 1, nutrient-deprivation autophagy factor-1, ENDOPLASMIC RETICULUM INTERMEMBRANE SMALL PROTEIN 
This gene plays a role in the regulation of autophagy.
National Institutes of Health

Papers overview

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2019
2019
Inherited genetic variation influencing leukocyte telomere length provides a natural experiment for testing associations with… 
Highly Cited
2013
Highly Cited
2013
Mitochondria are emerging as important players in the transformation process of cells, maintaining the biosynthetic and energetic… 
Highly Cited
2013
Highly Cited
2013
Miner1 is a redox‐active 2Fe2S cluster protein. Mutations in Miner1 result in Wolfram Syndrome, a metabolic disease associated… 
Highly Cited
2012
Highly Cited
2012
To extend understanding of the genetic architecture and molecular basis of type 2 diabetes (T2D), we conducted a meta-analysis of… 
Highly Cited
2012
Highly Cited
2012
The CISD2 gene, which is an evolutionarily conserved novel gene, encodes a transmembrane protein primarily associated with the… 
Highly Cited
2010
Highly Cited
2010
Although the essential genes for autophagy (Atg) have been identified, the molecular mechanisms through which Atg proteins… 
Highly Cited
2009
Highly Cited
2009
CISD2, the causative gene for Wolfram syndrome 2 (WFS2), is a previously uncharacterized novel gene. Significantly, the CISD2… 
Highly Cited
2009
Highly Cited
2007
Highly Cited
2007
A single missense mutation was identified in a novel, highly conserved zinc-finger gene, ZCD2, in three consanguineous families…